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Efficacy and Safety of FIRTECH in Patients With Mild to Moderate Acute Low Back Pain
Efficacy and Safety of FIRTECH in Patients With Mild to Moderate Acute Low Back Pain

NCT05137041

CompletedPhase 3

Sponsor: Sanofi

Conditions: Low Back Pain

Interventions: ITP FIRTECH

Countries: Germany, Italy

Primary Objective: To assess the efficacy of the infrared therapy patch (ITP) FIRTECH for treating participants suffering from mild to moderate acute low back pain. Secondary Objectives: * To assess the efficacy of ITP FIRTECH on participant disability * To assess the efficacy of ITP FIRTECH on the degree of participant mobility * To assess the safety of ITP FIRTECH

Eligibility overview

Sex: ALL

Age: 18 Years to 65 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Participants suffering from mild to moderate acute low back pain
* Low back pain (lumbar back pain) is defined as pain in the back from the level of the lowest rib down to the gluteal fold
* Acute episode is defined as acute pain with less than 1 month duration
* With intensity less than or equal to 6 on 0-10 Numerical Rating Scale (NRS)

Exclusion Criteria:

* Participants suffering from any neurological pathology which could be responsible of the pain
* Participants suffering from leg pain irradiation
* Participants suffering from chronic lumbar pain of any etiology
* Participants with chronic arthrosis and neurological symptoms
* Participants experiencing recent significant trauma (i.e., injury related to a fall from a height or motor vehicle crash, or from a minor fall or heavy lifting in a participants with osteoporosis or possible osteoporosis)
* Participants with major or progressive motor or sensory deficit, new-onset bowel or bladder incontinence or urinary retention, loss of anal sphincter tone, saddle anesthesia, history of cancer metastatic to bone, and suspected spinal infection
* Participants clinically diagnosed with anxiety and/or depression
* Participants using any medication for their pain within the last 48 hours within enrollment into the study
* Participants taking any systemic medication for their pain within the last 24 hours (48 hours for diclofenac or corticosteroids)
* Participants currently using recreational or illicit drugs or with a recent history of drug or alcohol abuse or dependence
* Participants with any other medical condition that would interfere with efficacy and safety assessments based on investigator's judgment
* Participants having received non-pharmaceutical lower back pain treatment (physiotherapy, heat treatment or massage) within 12 hours prior to enrollment
* Participants having received spinal injection back pain treatment within 6 months prior to enrollment
* Participants having received surgery due to back pain or rehabilitation due to back pain in the last 12 months
* Participants with a known sensitivity to paracetamol
* Participants with known cutaneous hypersensitivity to plaster
* Participants participating in another clinical study within the past 30 days
* Participants who are pregnant or breastfeeding; contraception is mandatory
* Participants having damaged, non-intact, or scarred skin in or near the point of patch application
* Participants having a known skin sensitivity
* Participants having impaired blood circulation

The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.
Locations (7)
  • Bad Homburg, Germany
  • Leipzig, Germany
  • Munich, Germany
  • Weinheim, Germany
  • Taormina, Messina, Italy
  • Alessandria, Italy
  • Chieti, Italy